EP1563050A1 - Soap bars exhibiting antibacterial effectiveness and method of producing same - Google Patents
Soap bars exhibiting antibacterial effectiveness and method of producing sameInfo
- Publication number
- EP1563050A1 EP1563050A1 EP03783678A EP03783678A EP1563050A1 EP 1563050 A1 EP1563050 A1 EP 1563050A1 EP 03783678 A EP03783678 A EP 03783678A EP 03783678 A EP03783678 A EP 03783678A EP 1563050 A1 EP1563050 A1 EP 1563050A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- soap
- soap bar
- carbon atoms
- alkyl chain
- chain lengths
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000344 soap Substances 0.000 title claims abstract description 192
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims description 21
- 230000001747 exhibiting effect Effects 0.000 title description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 45
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 235000021588 free fatty acids Nutrition 0.000 claims abstract description 18
- 239000007864 aqueous solution Substances 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims description 95
- 230000009467 reduction Effects 0.000 claims description 32
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 26
- 239000000194 fatty acid Substances 0.000 claims description 26
- 229930195729 fatty acid Natural products 0.000 claims description 26
- 150000004665 fatty acids Chemical class 0.000 claims description 25
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 21
- 239000002904 solvent Substances 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 230000003472 neutralizing effect Effects 0.000 claims description 18
- 230000008569 process Effects 0.000 claims description 13
- 241000894006 Bacteria Species 0.000 claims description 11
- 239000004615 ingredient Substances 0.000 claims description 10
- 241000588724 Escherichia coli Species 0.000 claims description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- 239000008149 soap solution Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- -1 pH adjusters Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
- 239000002671 adjuvant Substances 0.000 claims description 4
- 241000192125 Firmicutes Species 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 3
- 239000003205 fragrance Substances 0.000 claims description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 2
- 150000005215 alkyl ethers Chemical class 0.000 claims description 2
- 239000002738 chelating agent Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 2
- 235000011187 glycerol Nutrition 0.000 claims description 2
- SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920001451 polypropylene glycol Polymers 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 150000005846 sugar alcohols Chemical class 0.000 claims description 2
- 238000009472 formulation Methods 0.000 description 54
- 238000012360 testing method Methods 0.000 description 18
- 239000000243 solution Substances 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000001580 bacterial effect Effects 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 239000003242 anti bacterial agent Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002054 inoculum Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 239000006150 trypticase soy agar Substances 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005267 amalgamation Methods 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000030833 cell death Effects 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000013048 microbiological method Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000007793 ph indicator Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/006—Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/007—Soaps or soap mixtures with well defined chain length
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/26—Organic compounds, e.g. vitamins containing oxygen
Definitions
- the present invention relates generally to soap bars exhibiting antibacterial effectiveness and methods of producing the same, and more particularly to soap bars including soap components exhibiting antibacterial properties.
- Antibacterial personal care compositions are known in the art. Especially useful are antibacterial cleansing compositions, such as soap bars, that typically are used to cleanse the skin and to destroy bacteria and other microorganisms present on the skin, especially the hands, arms, and face of the user. Antibacterial compositions are used, for example, in the health care industry, food service industry, meat processing industry, and in the private sector by individual consumers. The widespread use of antibacterial compositions indicates the importance that consumers place on controlling bacteria and other microorganism populations on skin.
- soap bars conventionally comprise one or more "soaps", which, for purposes of describing this component of the soap bars of the present invention, has the meaning as normally understood in the art: monovalent salts of monocarboxylic fatty acids.
- the counterions of the salts generally include sodium, potassium, ammonium and alkanolammonium ions, but may include other suitable ions known in the art.
- the soap bars also may include optional adjuvant ingredients such as moisturizers, humectants, water, fillers, polymers, dyes, fragrances and the like to effect cleansing and/or conditioning for the skin of the user.
- the soap components in conventional soap bars comprise salts of long chain fatty acids having chain lengths of the alkyl group of the fatty acid from about 12 carbon atoms to about 18 carbon atoms in length.
- the particular length of the alkyl chain(s) of the soaps is selected for various reasons, including cleansing capability, lather capability, costs, and the like. It is known that soaps of shorter chain lengths are more water-soluble (i.e., less hydrophobic) and produce more lather compared to longer chain length soaps. Longer chain length soaps are often selected for cost reasons and to provide structure to the soap bars.
- the soap bars in accordance with various aspects of the present invention exhibit antibacterial effectiveness due to the antibacterial properties of the soap components comprising the bars, separate and distinct from any added antibacterial active agents.
- Such soap bars have surprising antibacterial effectiveness at relatively short contact times compared to conventional soap bars that typically comprise soap compositions of salts having
- a soap bar that exhibits antibacterial effectiveness comprises, by weight at least about 50% soap having alkyl chain lengths of 8-10 carbon atoms, water, about 10% to about 30% hydric solvent, preferably about
- a soap bar that comprises, by weight, at least about 50% soap having alkyl chain lengths of 8-10 carbon atoms.
- the soap bar exhibits a log reduction against Gram positive bacteria of at least 3 after 30 seconds of contact at 40°C, as measured against S. aureus.
- a method of making a soap bar that exhibits antibacterial effectiveness comprises, by weight, at least about 50% soap having alkyl chain lengths of 8-10 carbon atoms, and water.
- the process comprises combining a neutralizing agent and fatty acids having alkyl chain lengths of 8-10 carbon atoms to form a soap solution and manipulating the composition of the soap solution, if necessary, so that a pH of a 10% aqueous solution of the soap bar is no greater than about 9.
- the process further includes removing a portion of water from the soap solution, optionally adding adjuvant ingredients, and solidifying to form the soap bar.
- the soap bars comprise at least about 45%, and preferably about 50%, by weight, of salts of monocarboxylic fatty acids having alkyl chains of 8 carbon atoms (C8), or 10 carbon atoms (CIO), or a mixture of salts having alkyl chains of 8 and 10 carbon atoms.
- Counterions of the salts may include sodium, potassium, ammonia and alkanolammonium ions, although sodium is generally the preferred counterion.
- the soap bars comprise less than 1.5%, preferably less than 1%, by weight, of salts of monocarboxylic fatty acids having alkyl chains of 12 (C12) to 16 (C16) carbon atoms, as
- salts of monocarboxylic fatty acids having alkyl chains of 12 to 16 carbon atoms are substantially completely absent from the soap bars of the present invention.
- the soap bars are formed to comprise a free acid content such that a 10% aqueous solution of a soap bar of the present invention has a pH no greater than about 9.5, preferably no greater than about 9.
- the soap molecules formed in accordance with embodiments of the present invention provide more free monomers in solution than longer chain soap molecules.
- the soap bars comprise compositions which assist in the formation of solutions and/or prevent or reduce formation of dispersions.
- the soap bars comprise a hydric solvent, preferably about 10% to about 30% by weight, and most preferably on the order of about 20% by weight.
- the hydric solvent may comprise any now known or hereafter devised solvent, for example, an exemplary hydric solvent includes propylene glycol.
- the soap bars may comprise minor amounts, preferably no more than 5% by weight, of salts of monocarboxylic fatty acids having alkyl chains of 18 (C18) or more carbon atoms to provide structure in the finished soap bars and prevent or retard disintegration of the soap bar on exposure to water.
- the soap bars may be formed using water-soluble polyhydric organic solvents.
- Polyhydric organic solvents suitable for use in producing soap bars in accordance with the various embodiments of the present invention include, but are not limited to, propylene glycol, dipropylene glycol, butylene glycol, ethylene glycol, 1,7- heptanediol, monoethylene glycols, polyethylene glycols, polypropylene glycols of up to 8,000 molecular weight, mono-Cl-4 alkyl ethers of any of the foregoing, mixtures thereof, glycerine, and any sugar alcohol, such as, for example, sorbitol.
- the soap bars in accordance with the present invention may also contain other optional adjuvant ingredients that are present in sufficient amount to perform their intended function and that do not adversely affect the antibacterial efficacy of the soap bar composition.
- Such optional ingredients typically are present, individually, from about 0% to about 2%, by weight of the soap bar, and, collectively, from 0% to about 10%, by weight of the soap bar.
- Classes of optional ingredients may include, but are not limited to, dyes, fragrances, pH adjusters, chelating agents, preservatives, stabilizers, colorants, polymers such as synthetic high polymers, derivatives of natural polymers such as modified cellulosic polymers, gums, and the like, antibacterial active agents, and similar classes of optional ingredients known the art.
- the soap components of the soap bars may be manufactured by mixing a fatty acid or acids and at least one neutralizing agent in an open agitated reaction vessel at atmospheric pressure and heating to a temperature sufficient to melt the fatty acids, generally at least about 80°C to 90°C.
- the fatty acids include monocarboxylic fatty acids having alkyl chain lengths of 8 carbon atoms (C8) or 10 carbon atoms (CIO), or a mixture of such fatty acids.
- Suitable neutralizing agents for manufacturing of the soap bars of the present invention include caustic solutions, for example, sodium bases such as NaOH.
- the neutralizing agent neutralizes the fatty acids, forming salts of the fatty acids (i.e., "soaps"), such as for example, sodium, potassium, ammonia or alkanolammonium salts.
- the neutralizing agent may be added in an amount less than the amount of the neutralizing agent required to fully neutralize the fatty acids. In one exemplary embodiment of the invention, about 95% of the required amount of neutralizing agent needed to fully neutralize the fatty acids may be added.
- the temperature preferably is maintained above about 80°C but below about 100°C. Additionally, a hydic solvent, such as propylene glycol, may be added to the mixture.
- the mixture should comprise, preferably about 10% to about 30% hydric solvent by weight, and most preferably on the order of about 20% by weight.
- the hydric solvent may comprise any now known or hereafter devised solvent.
- the mixture may be analyzed for free acid and the pH of the mixture manipulated accordingly.
- the mixture may be titrated with NaOH using a pH indicator and, if necessary, the composition of the mixture may be manipulated so that a 10% aqueous solution of the resulting soap bar has a pH no greater than about 9.
- the pH is too acidic, more neutralizing agent may be added.
- the mixture has a pH above about 9, more free fatty acids may be added to the composition. If free fatty acids are added, it is preferable that the free fatty acids have alkyl chains of 8 to 10 carbon atoms.
- the temperature of the reaction mixture may be raised to at least about 90°C, preferably from about 90°C to about 100°C, to evaporate a desired amount of water.
- the water may be evaporated before addition of an additional neutralizing agent or free fatty acid as described above.
- the soap bar comprises no more than 25 % water.
- the soap bar comprises no more than 20% water. More preferably, the soap bar comprises no more than 15% water.
- the soap component When a desired amount of water has been removed from the soap component, the soap component may be cooled, optional ingredients may be added to the soap component using conventional methods, and the resulting composition may be formed into soap bars, either by pouring the composition, in a molten state, into molds, or, alternatively, by forming soap bars using conventional amalgamation, milling, plodding and/or stamping procedures as is well known in the art.
- the soap bars may be made with a solvent.
- the above-described process may be used, except that a polyhydric solvent is initially added to the reaction vessel and heated to a temperature of about 70°C to 80°C.
- the neutralizing agent is then added to the solvent before the addition of the fatty acids(s) to prevent formation of gels or lumps, which would increase manufacturing time.
- the neutralizing agent is added in an amount less than the amount of the neutralizing agent required to fully neutralize the later-added fatty acids. In one exemplary embodiment of the invention, about 95% of the required amount of neutralizing agent needed to fully neutralize the fatty acids is added.
- time kill suspension tests were conducted, whereby the survival of challenged organisms exposed to an antibacterial test formulation is determined as a function of time.
- the time kill method is well known in the antibacterial products industry. In this test method, a diluted aliquot of the formulation is brought into contact with a known population of test bacteria for a specified time period at a specified temperature.
- test composition is neutralized at the end of the time period, which arrests the antibacterial activity of the composition.
- percent or, alternatively, log reduction from the original bacteria population is calculated. All testing is generally performed in triplicate, the results are combined, and the average log reduction is reported.
- the choice of contact time period is at the discretion of the investigator. Any contact time period can be chosen. Typical contact times range from 15 seconds to 5 minutes, with 30 seconds and 1 minute being typical contact times.
- the bacterial suspension, or test inoculum is prepared by growing a bacterial culture on any appropriate solid media (e.g., agar).
- the bacterial population then is washed from the agar with sterile physiological saline and the population of the bacterial suspension is adjusted to about 10 8 colony-forming units per ml (cfu/ml).
- the table below lists the test bacterial cultures used in the following tests and includes the name of the bacteria, the ATCC (American Type Culture Collection) identification number, and the abbreviation for the name of the organism used hereafter.
- S. aureus is a Gram positive bacteria
- E. coli is a Gram negative bacteria.
- EXAMPLE 1 In this example, five different formulations of soap bars were tested using the time kill suspension test method. Table 1 summarizes the compositions of three formulations, Formulations 1A, IB, and IC. Two formulations (Formulations 1A and IB) were formed in accordance with various aspects of the present invention. The third formulation (Formulation IC) was formed with soap having alkyl chain lengths not in accordance with various aspects of the present invention. These three formulations, with each of the components set forth in weight percent, are as follows:
- the five different formulations were tested using 10% aqueous solutions of the formulations. Each solution was added to a beaker in a water bath, stirred, and heated to approximately 40°C, which is typically the temperature at which consumers use soap bars for body cleansing. The solution then was inoculated with 1.0 ml of the test bacteria suspensions. The inoculum was stirred with the solution for a contact time of 30 seconds and 1 minute.
- the plate counts were converted to cfu/ml for the numbers control and samples, respectively, by standard microbiological methods.
- the log reduction or, alternatively, the percent reduction, in bacterial populations provided by the antibacterial composition correlates to antibacterial activity.
- a log reduction of 3-5 is most preferred, a 1-3 reduction is preferred, whereas a log reduction of less than 1 is least preferred, for a particular contact time.
- a highly preferred antibacterial composition exhibits a 3-5 log reduction against a broad spectrum of microorganisms in a short contact time.
- Table 2 summarizes the results of time kill tests performed on the solutions of the five formulations at 30 seconds and 1 minute contact times:
- Formulations 1A and IB exhibited superior antibacterial effectiveness against S. aureus compared to Formulation IC, Formulation ID, and Formulation IE. Both Formulations 1A and IB exhibited log reductions of between 3 and 5, while the other formulations exhibited log reductions of only between 2 and 3.
- Formulation 1A which comprised a mixture of NaC8 and NaCIO soaps, exhibited particularly good antibacterial effectiveness, with a log reduction of between 4 and 5.
- Formulations 1A and IB exhibited superior antibacterial effectiveness against E. coli compared to Formulation ID and Formulation IE. Both Formulations 1A and IB exhibited log reductions of between 4 and 5, while the other two formulations exhibited log reductions of less than 1.
- the antibacterial effectiveness against E. coli of Formulation IC was the same as Formulations 1A and IB.
- Formulation IE which exhibited a log reduction of less than 1.
- EXAMPLE 2 Further testing was conducted to compare the antibacterial effectiveness of soap bars formed in accordance with various aspects of the present invention with soap bars that do not have the free fatty acid content contemplated by various aspects of the present invention.
- Four different formulations of soap bars were tested with the time kill suspension test method described above using an S. aureus test inoculum.
- Formulations 2A and 2C comprised 28.8% NaC8, 28.2% NaCIO, 33.5 % propylene glycol and the balance water.
- Formulations 2B and 2D comprised 28.8% NaC8, 28.2% NaCIO, 33.4 % propylene glycol and the balance water.
- soap bars in accordance with various aspects of the present invention that is, soap bars of C8 and CIO soaps formed to comprise an amount of free fatty acid such that the pH of a 10% aqueous solution of the soap bar has a pH no greater than about 9, exhibit substantially higher antibacterial effectiveness than soap bars of C8 and CIO soaps with less free fatty acid.
- Formulation 2A and 2B both tested at 40°C
- Formulation 2A exhibited a log reduction of greater than 3
- Formulation 2B exhibited a log reduction of less than 2.
- soap bars formed in accordance with the present invention work particularly well at temperatures at which consumers are generally likely to use the soap bars for body cleansing. Comparing Formulations 2A and 2C, each with a pH of 8.6, Formulation 2A tested at 40°C exhibited a log reduction of greater than 3, while Formulation 2C tested at 25°C exhibited a log reduction less than 2.
- soap bars in accordance with the various embodiments of the present invention evidence enhanced antibacterial effectiveness due to the composition of the soap components comprising the soap bars, separate and distinct from any added antibacterial agent. Accordingly the soap bars in accordance with various embodiments of the present invention may constitute effective, yet low-cost, antibacterial soap bars.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US300266 | 1994-09-02 | ||
| US10/300,266 US6794344B2 (en) | 2002-11-20 | 2002-11-20 | Soap bars exhibiting antibacterial effectiveness and method of producing same |
| PCT/US2003/036947 WO2004046294A1 (en) | 2002-11-20 | 2003-11-19 | Soap bars exhibiting antibacterial effectiveness and method of producing same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1563050A1 true EP1563050A1 (en) | 2005-08-17 |
| EP1563050B1 EP1563050B1 (en) | 2012-04-11 |
Family
ID=32297884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP03783678A Expired - Lifetime EP1563050B1 (en) | 2002-11-20 | 2003-11-19 | Soap bars exhibiting antibacterial effectiveness and method of producing same |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6794344B2 (en) |
| EP (1) | EP1563050B1 (en) |
| AT (1) | ATE553178T1 (en) |
| AU (1) | AU2003291090A1 (en) |
| WO (1) | WO2004046294A1 (en) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2603403A1 (en) * | 2005-04-01 | 2006-10-12 | Zymes, Llc | Skin enrichment using coq10 as the delivery system |
| AU2006322383B2 (en) * | 2005-12-07 | 2010-03-11 | Unilever Plc | Improved detergent composition |
| US9549550B2 (en) | 2009-10-30 | 2017-01-24 | David Changaris | Method and composition for long acting bacterial suppression on skin |
| CA2908910C (en) | 2013-04-16 | 2021-03-02 | Unilever Plc | Liquid soap having enhanced antibacterial activity |
| JP6577937B2 (en) * | 2013-04-16 | 2019-09-18 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Bar soap with improved antibacterial activity |
| WO2019120905A1 (en) | 2017-12-21 | 2019-06-27 | Unilever N.V. | Fast-acting biocidal cleansing composition |
| CN112996895A (en) * | 2018-11-12 | 2021-06-18 | 联合利华知识产权控股有限公司 | Extruded soap bars with enhanced antimicrobial efficacy |
| US11414632B2 (en) | 2019-03-01 | 2022-08-16 | Conopco, Inc. | Soap bar with improved perfume impact and deposition of actives |
| MX2021010271A (en) | 2019-03-01 | 2021-09-23 | Unilever Ip Holdings B V | Bar compositions comprising c10 soap while minimizing ratio of unsaturated c18 soap to caprate. |
| US20250049666A1 (en) | 2021-12-27 | 2025-02-13 | Conopco Inc., D/B/A Unilever | Liquid composition having enhanced antimicrobial activity |
| CN118829714A (en) | 2021-12-27 | 2024-10-22 | 联合利华知识产权控股有限公司 | Bar compositions with enhanced antimicrobial activity |
| CN118043442A (en) | 2022-08-12 | 2024-05-14 | 宝洁公司 | Solid soluble compositions |
| WO2024036124A1 (en) | 2022-08-12 | 2024-02-15 | The Procter & Gamble Company | Solid dissolvable compositions |
| MX2024006599A (en) | 2022-08-12 | 2024-06-12 | Procter & Gamble | Solid dissolvable compositions. |
| WO2024036120A1 (en) | 2022-08-12 | 2024-02-15 | The Procter & Gamble Company | Solid dissolvable compositions |
| CN117940547A (en) * | 2022-08-12 | 2024-04-26 | 宝洁公司 | Solid soluble composition |
| WO2024141375A1 (en) | 2022-12-27 | 2024-07-04 | Unilever Ip Holdings B.V. | Translucent or transparent isotropic liquid wash composition |
| EP4642426A1 (en) | 2022-12-27 | 2025-11-05 | Unilever IP Holdings B.V. | Isotropic liquid wash composition with esterified nonionic thickener |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE420383A (en) * | 1937-02-25 | |||
| BE446235A (en) * | 1945-07-11 | |||
| US5021183A (en) * | 1986-10-27 | 1991-06-04 | Abel Saud | Soap composition |
| GB2235930A (en) * | 1989-09-12 | 1991-03-20 | Unilever Plc | Soap composition |
| GB2243615B (en) * | 1990-05-04 | 1993-03-31 | Procter & Gamble | Beta-phase soap bars including those containing low level of moisture and solubilized solid antibacterial agent |
| US5874392A (en) * | 1996-05-09 | 1999-02-23 | Halvorson; Raymond George | Soap |
| US6007831A (en) | 1998-01-08 | 1999-12-28 | Lever Brothers Company | Soap bars having quick kill capacity and methods of enhancing such capacity |
| GB9803771D0 (en) * | 1998-02-23 | 1998-04-15 | Unilever Plc | Soap bar |
| US6143704A (en) * | 1998-10-13 | 2000-11-07 | Lever Brothers Company, Division Of Conopco, Inc. | Soap bars with little or no synthetic surfactant comprising organic salts |
| US6107261A (en) * | 1999-06-23 | 2000-08-22 | The Dial Corporation | Compositions containing a high percent saturation concentration of antibacterial agent |
| US6310015B1 (en) * | 1999-08-10 | 2001-10-30 | The Dial Corporation | Transparent/translucent moisturizing/cosmetic/personal cleansing bar |
| US6342470B1 (en) * | 2000-04-26 | 2002-01-29 | Unilever Home & Personal Care Usa | Bar comprising soap, fatty acid, polyalkylene glycol and protic acid salts in critical ratios and providing enhanced skin care benefits |
-
2002
- 2002-11-20 US US10/300,266 patent/US6794344B2/en not_active Expired - Lifetime
-
2003
- 2003-11-19 EP EP03783678A patent/EP1563050B1/en not_active Expired - Lifetime
- 2003-11-19 WO PCT/US2003/036947 patent/WO2004046294A1/en not_active Ceased
- 2003-11-19 AU AU2003291090A patent/AU2003291090A1/en not_active Abandoned
- 2003-11-19 AT AT03783678T patent/ATE553178T1/en active
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2004046294A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US6794344B2 (en) | 2004-09-21 |
| WO2004046294A1 (en) | 2004-06-03 |
| ATE553178T1 (en) | 2012-04-15 |
| US20040097387A1 (en) | 2004-05-20 |
| EP1563050B1 (en) | 2012-04-11 |
| AU2003291090A1 (en) | 2004-06-15 |
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